ENST00000302850.10:c.3232A>G
MANE Select
|
ENSP00000303830.4:p.Met1078Val
|
|
ENST00000302850.9:c.3232A>G
|
ENSP00000303830.4:p.Met1078Val
|
|
ENST00000341500.9:c.3196A>G
|
ENSP00000342838.4:p.Met1066Val
|
|
ENST00000593970.1:n.78A>G
|
|
|
NM_000208.2:c.3232A>G
|
NP_000199.2:p.Met1078Val
|
|
NM_000208.3:c.3232A>G
|
NP_000199.2:p.Met1078Val
|
|
NM_001079817.1:c.3196A>G
|
NP_001073285.1:p.Met1066Val
|
|
NM_001079817.2:c.3196A>G
|
NP_001073285.1:p.Met1066Val
|
|
XM_011527988.1:c.3307A>G
|
XP_011526290.1:p.Met1103Val
|
|
XM_011527989.1:c.3271A>G
|
XP_011526291.1:p.Met1091Val
|
|
XM_011527988.2:c.3229A>G
|
XP_011526290.2:p.Met1077Val
|
|
XM_011527989.3:c.3193A>G
|
XP_011526291.2:p.Met1065Val
|
|
NM_000208.4:c.3232A>G
MANE Select
|
NP_000199.2:p.Met1078Val
|
|
NM_001079817.3:c.3196A>G
|
NP_001073285.1:p.Met1066Val
|
|